New learning discoveries about Indolin-2-one

Category: indolines-derivatives. Feng, JX; Huang, Y in [Feng, Jiaxu; Huang, You] Nankai Univ, Coll Chem, State Key Lab, Tianjin 300071, Peoples R China; [Feng, Jiaxu; Huang, You] Nankai Univ, Coll Chem, Inst Elementoorgan Chem, Tianjin 300071, Peoples R China published Phosphine-Catalyzed Remote 1,7-Addition for Synthesis of Diene Carboxylates in 2020.0, Cited 105.0. The Name is Indolin-2-one. Through research, I have a further understanding and discovery of 59-48-3.

Category: indolines-derivatives. Feng, JX; Huang, Y in [Feng, Jiaxu; Huang, You] Nankai Univ, Coll Chem, State Key Lab, Tianjin 300071, Peoples R China; [Feng, Jiaxu; Huang, You] Nankai Univ, Coll Chem, Inst Elementoorgan Chem, Tianjin 300071, Peoples R China published Phosphine-Catalyzed Remote 1,7-Addition for Synthesis of Diene Carboxylates in 2020.0, Cited 105.0. The Name is Indolin-2-one. Through research, I have a further understanding and discovery of 59-48-3.

A phosphine-catalyzed remote 1,7-addition of vinyl allenoates has been developed, providing a series of 1,3-dienes derivatives in high yields (up to 99%) and with good chemo-, regio-, and stereoselectivity. This reaction demonstrated that the introduction of vinyl in allenoates effectively extended reaction types of phosphine-catalyzed nucleophilic addition of allenoates, leading to concise synthesis of diene carboxylates. Notably, the enantioselective variant of this 1,7-addition can also be performed by chiral phosphine catalyst.

Category: indolines-derivatives. Welcome to talk about 59-48-3, If you have any questions, you can contact Feng, JX; Huang, Y or send Email.

Reference:
Indoline – Wikipedia,
,Indoline | C8H9N – PubChem